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Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Tofacitinib temporarily regrew hair in a man with alopecia, but its effects didn't last.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

New genes and pathways are important for testosterone production and male sexual development.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Six new hair loss factors in men not linked to female hair loss.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.